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Ensuring ISO 17025:2017 Compliance in Your Laboratory

: 12 Jun 2019

Sector: Laboratory Equipment, Pharmaceutical

Type: Webinar


Learn how a LIMS can help support the requirements of ISO/IEC 17025:2017.

 

A cornerstone of the third edition of the ISO/IEC 17025 (ISO/IEC17025:2017) standard is the requirement for laboratories to demonstrate they operate competently and are able to generate valid results. This, in turn, is key to building trust in the quality of the data and information provided to partners, customers and collaborators.

 

While ISO/IEC 17025:2017 emphasizes a risk-based approach over prescribed working practices, it is still a management system that must be defined, implemented and shown to be adhered to.

 

This Webinar discusses how a well implemented Laboratory Information Management System can support many aspects of an ISO/IEC 17025:2017 based management system, over and above just the technical records (Section 7.5). It will illustrate how workflow definition and process enforcement aid adherence to an ISO/IEC 17025:2017 management system and discusses the benefits of an integrated information management system strategy.

 

This webinar will cover a number of aspects of how LIMS supports ISO 17025, among them;

  • Data Integrity/Result Validity
  • Measurement Uncertainty and Limits
  • Instrument Calibration and Maintenance
  • SOP and document management
  • CAPA management
  • Monitoring of environmental conditions for potential contamination

 

Discover how a LIMS can help your Laboratory meet the needs of 17025:2017

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